Nursing Elites

1. Which of the following is the weakest intermolecular force?

• A. Dipole interactions
• B. Hydrogen bonding
• C. Van der Waals forces
• D. Dispersion forces

Correct answer: D

Rationale: Dispersion forces, also known as London dispersion forces, are the weakest intermolecular forces. They are temporary attractive forces that occur due to momentary shifts in electron distribution within molecules. While dipole interactions, hydrogen bonding, and Van der Waals forces are stronger intermolecular forces, dispersion forces are the weakest because they arise from short-lived fluctuations in electron density. Dipole interactions involve permanent dipoles in molecules, making them stronger than dispersion forces. Hydrogen bonding is stronger than dipole interactions and involves hydrogen atoms bonded to highly electronegative atoms. Van der Waals forces encompass dipole-dipole interactions and dispersion forces, making them stronger than dispersion forces alone.

2. What is the chemical reaction that involves breaking down a compound into component parts?

• A. Decomposition
• B. Synthesis
• C. Combustion
• D. Single replacement

Correct answer: A

Rationale: Decomposition is the correct answer because in a decomposition reaction, a compound is broken down into simpler substances. This type of reaction involves the splitting of a compound into its component parts, often through the use of heat, light, or electricity. Synthesis (choice B) is the opposite process where simpler substances are combined to form a more complex compound. Combustion (choice C) is a reaction involving rapid oxidation often accompanied by heat and light. Single replacement (choice D) is a reaction where one element replaces another in a compound.

3. What charge do Group IA elements have?

• A. +1
• B. +2
• C. +3
• D. 0

Correct answer: A

Rationale: Group IA elements, also known as alkali metals, have a +1 charge. They readily lose one electron to achieve a stable electron configuration, forming ions with a single positive charge. This makes +1 the correct choice. Choices B, C, and D are incorrect because alkali metals in Group IA typically lose one electron, so they do not have a +2, +3, or 0 charge.

4. What color does phenolphthalein turn in the presence of an acid?

• A. Clear
• B. Blue
• C. Pink
• D. Red

Correct answer: C

Rationale: In the presence of an acid, phenolphthalein turns pink. Phenolphthalein is a pH indicator that is colorless in acidic solutions but turns pink in basic solutions. Therefore, when added to an acidic solution, phenolphthalein will exhibit a pink coloration. Choice A, 'Clear,' is incorrect because phenolphthalein does not remain colorless in the presence of an acid. Choice B, 'Blue,' is incorrect as phenolphthalein does not turn blue in the presence of an acid. Choice D, 'Red,' is incorrect as phenolphthalein does not exhibit a red color in acidic solutions.

5. What is the name of the compound CH₃-CH₂-CH₂-CH₃?

• A. Cyclobutane
• B. Butane
• C. Butene
• D. Butyne

Correct answer: B

Rationale: The compound CH₃-CH₂-CH₂-CH₃ is named butane. Butane is a straight-chain alkane comprising four carbon atoms connected by single bonds. The prefix 'but-' denotes the presence of four carbon atoms, while the suffix '-ane' indicates it is an alkane with single bonds between the carbon atoms. Choice A, Cyclobutane, is incorrect as it refers to a cyclic hydrocarbon with four carbon atoms in a ring structure. Choice C, Butene, is incorrect because it is an alkene with a double bond between two carbon atoms, not a saturated hydrocarbon like butane. Choice D, Butyne, is also incorrect as it is an alkyne with a triple bond between two carbon atoms, unlike the single bonds in butane.

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